ATA70979A - METHOD FOR PRODUCING NEW 1-SUBSTITUTED IMIDAZOLE DERIVATIVES AND THEIR SALTS - Google Patents
METHOD FOR PRODUCING NEW 1-SUBSTITUTED IMIDAZOLE DERIVATIVES AND THEIR SALTSInfo
- Publication number
- ATA70979A ATA70979A AT0070979A AT70979A ATA70979A AT A70979 A ATA70979 A AT A70979A AT 0070979 A AT0070979 A AT 0070979A AT 70979 A AT70979 A AT 70979A AT A70979 A ATA70979 A AT A70979A
- Authority
- AT
- Austria
- Prior art keywords
- salts
- imidazole derivatives
- substituted imidazole
- producing new
- producing
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/485—Morphinan derivatives, e.g. morphine, codeine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/16—Preparation of halogenated hydrocarbons by replacement by halogens of hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/84—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/10—1,4-Dioxanes; Hydrogenated 1,4-dioxanes
- C07D319/14—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
- C07D319/16—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D319/20—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring with substituents attached to the hetero ring
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicinal Preparation (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT184583A AT378772B (en) | 1978-02-01 | 1983-05-19 | METHOD FOR PRODUCING NEW 1-SUBSTITUTED IMIDAZOLE DERIVATIVES AND THEIR SALTS |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB398478 | 1978-02-01 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| ATA70979A true ATA70979A (en) | 1983-04-15 |
| AT372949B AT372949B (en) | 1983-11-25 |
Family
ID=9768613
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT0070979A AT372949B (en) | 1978-02-01 | 1979-01-31 | METHOD FOR PRODUCING NEW 1-SUBSTITUTED IMIDAZOLE DERIVATIVES AND THEIR SALTS |
Country Status (26)
| Country | Link |
|---|---|
| US (2) | US4416895A (en) |
| EP (2) | EP0003732B1 (en) |
| JP (1) | JPS54145665A (en) |
| AT (1) | AT372949B (en) |
| AU (1) | AU533272B2 (en) |
| BE (1) | BE873849A (en) |
| CA (2) | CA1146549A (en) |
| CH (1) | CH643736A5 (en) |
| DE (3) | DE2862340D1 (en) |
| DK (1) | DK41479A (en) |
| ES (1) | ES477305A1 (en) |
| FI (1) | FI790314A7 (en) |
| FR (2) | FR2416012A1 (en) |
| GB (2) | GB2018136B (en) |
| GR (1) | GR65609B (en) |
| HU (1) | HU182629B (en) |
| IE (1) | IE47649B1 (en) |
| IL (1) | IL56556A (en) |
| IT (1) | IT1115800B (en) |
| LU (1) | LU80863A1 (en) |
| MC (1) | MC1241A1 (en) |
| NL (1) | NL7900807A (en) |
| NZ (1) | NZ189520A (en) |
| PT (1) | PT69165A (en) |
| SE (1) | SE7900834L (en) |
| ZA (1) | ZA79412B (en) |
Families Citing this family (60)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55313A (en) * | 1978-06-13 | 1980-01-05 | Kissei Pharmaceut Co Ltd | Imidazole derivative |
| DK75680A (en) * | 1979-02-22 | 1980-08-23 | Wellcome Found | PROCEDURE FOR THE PREPARATION OF 1-SUBSTITUTED IMIDAZOLS |
| GR73560B (en) * | 1979-02-24 | 1984-03-15 | Pfizer | |
| DK157860C (en) * | 1979-06-07 | 1990-07-30 | Shionogi & Co | METHOD OF ANALOGUE FOR THE PREPARATION OF BENZYLIMIDAZOLD DERIVATIVES AND PHARMACEUTICAL ACCEPTABLE ACID ADDITION SALTS THEREOF |
| US4218461A (en) * | 1979-08-15 | 1980-08-19 | E. R. Squibb & Sons, Inc. | 2,3-Dihydro-2-[(1H-imidazol-1-yl)-methylene]-1H-inden-1-ones |
| PH16249A (en) * | 1980-02-04 | 1983-08-16 | Reckitt & Colmann Prod Ltd | Imidazoline derivatives,its pharmaceutical composition and method of use |
| US4321272A (en) * | 1980-08-25 | 1982-03-23 | Syntex (U.S.A.) Inc. | Derivatives of substituted N-alkylimidazoles |
| NL8005204A (en) * | 1980-09-17 | 1982-04-16 | Gist Brocades Nv | ETHENYL-IMIDAZOLE DERIVATIVES WITH ANTIMYCOTIC EFFICACY. |
| GR75101B (en) * | 1980-10-23 | 1984-07-13 | Pfizer | |
| JPS6036427B2 (en) * | 1980-12-05 | 1985-08-20 | 塩野義製薬株式会社 | 1-benzylimidazole derivative |
| DE3103068A1 (en) * | 1981-01-30 | 1982-08-26 | Basf Ag, 6700 Ludwigshafen | VINYLAZOLE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE IN FIGHTING FUNGI |
| ZA824343B (en) * | 1981-07-01 | 1983-04-27 | Upjohn Co | Pyridinyl- and imidazolyl-benzofurane and benzothiophenes |
| ZA825413B (en) * | 1981-08-26 | 1983-06-29 | Pfizer | Thromboxane synthetase inhibitors, processes for their production, and pharmaceutical compositions comprising them |
| GB2115408B (en) * | 1982-02-09 | 1985-10-16 | Ici Plc | Triazole and imidazole derivatives |
| EP0091503A1 (en) * | 1982-04-14 | 1983-10-19 | Gist-Brocades N.V. | Process of combatting fungal infections |
| CA1212115A (en) * | 1982-08-14 | 1986-09-30 | Peter B. Thorogood | Imidazole derivatives and salts thereof, their synthesis, and pharmaceutical formulations |
| JPS59225183A (en) * | 1983-02-01 | 1984-12-18 | Yoshitomi Pharmaceut Ind Ltd | Dihydrobenzofuran derivative |
| DE3484023D1 (en) * | 1983-03-03 | 1991-03-07 | Basf Ag | AZOLYLMETHYLCYCLOALKANE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A MEDICINAL PRODUCT. |
| US4536505A (en) * | 1983-05-17 | 1985-08-20 | Ciba-Geigy Corporation | Certain N-(pyridyl) indoles |
| PH22076A (en) * | 1983-08-25 | 1988-05-20 | Daiichi Seiyaku Co | Benzocycloalkane derivative |
| IT1212791B (en) * | 1983-11-24 | 1989-11-30 | Medea Res Srl | IMIDAZOLIC DERIVATIVES VASODILATOR AND ANTITROMBOTIC ADAPTITY, ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN IT. |
| US4690942A (en) * | 1983-12-20 | 1987-09-01 | Ciba-Geigy Corporation | 1-aryl-2-fluoro-2-azolyl alkanones, alkanols, esters, and ethers, composition containing them, and use of them to control phytopathogenic microorganisms |
| EP0149976A3 (en) * | 1983-12-30 | 1986-12-10 | Ciba-Geigy Ag | Substituted imidazoles |
| US4593029A (en) * | 1984-02-15 | 1986-06-03 | Syntex (U.S.A.) Inc. | Novel ω-(N-imidazolyl)alkyl ethers of 1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-2-ones |
| US4659730A (en) * | 1984-06-18 | 1987-04-21 | Eli Lilly And Company | Aromatase inhibiting imidazole derivatives |
| US4609733A (en) * | 1984-12-27 | 1986-09-02 | Ciba-Geigy Corporation | 3-keto-substituted-N-pyridylindoles |
| DE3508905A1 (en) * | 1985-03-13 | 1986-09-18 | Hoechst Ag, 6230 Frankfurt | NEW IMIDAZOLYL COMPOUNDS AND METHOD FOR THEIR PRODUCTION |
| IL81264A (en) * | 1986-01-30 | 1990-11-05 | Takeda Chemical Industries Ltd | Quinone derivatives,their production and pharmaceutical compositions containing them |
| US5229385A (en) * | 1986-01-30 | 1993-07-20 | Takeda Chemical Industries, Ltd. | Quinone derivatives, their production and use |
| US4749713A (en) * | 1986-03-07 | 1988-06-07 | Ciba-Geigy Corporation | Alpha-heterocycle substituted tolunitriles |
| JP2581556B2 (en) * | 1986-05-06 | 1997-02-12 | メレルダウファーマスーティカルズ インコーポレーテッド | Novel dopamine beta-hydroxylase inhibitor |
| KR930004646B1 (en) * | 1986-12-09 | 1993-06-02 | 다나베 세이야꾸 가부시끼가이샤 | Pharmaceutical composition for prophylaxis and treatment of cardiac hypertrophy |
| EP0285356A3 (en) * | 1987-03-30 | 1989-05-31 | Smithkline Beecham Corporation | Dopamine-beta-hydroxylase inhibitors |
| US4837333A (en) * | 1987-05-14 | 1989-06-06 | G. D. Searle & Co. | Substituted alkylidene imidazoles |
| DE3811574A1 (en) * | 1988-03-31 | 1989-10-19 | Schering Ag | N-SUBSTITUTED IMIDAZOLES, METHODS FOR THEIR PRODUCTION AND THEIR USE IN MEDICINAL PRODUCTS |
| IL91542A0 (en) * | 1988-10-06 | 1990-04-29 | Erba Carlo Spa | N-imidazolyl-and n-imidazolyl-methyl derivatives of substituted bicyclic compounds,their preparation and pharmaceutical compositions containing them |
| JPH0710862B2 (en) * | 1989-08-08 | 1995-02-08 | 宇部興産株式会社 | Azolidine derivative, its manufacturing method and agricultural / horticultural fungicide |
| JPH03115267A (en) * | 1989-09-28 | 1991-05-16 | Maruho Kk | Propiophenone derivative, its production and central muscle relaxant and antispasmodic agent containing the same |
| US5073566A (en) * | 1989-11-30 | 1991-12-17 | Eli Lilly And Company | Angiotensin ii antagonist 1,3-imidazoles and use thereas |
| US5635521A (en) * | 1991-09-23 | 1997-06-03 | Sandoz Ltd. | Imidazolylmethyl-pyridines |
| DE4131584A1 (en) * | 1991-09-23 | 1993-03-25 | Sandoz Ag | IMIDAZOLYLMETHYL-PYRIDINE, THEIR PRODUCTION AND USE AS A PHARMACEUTICAL |
| MY110108A (en) * | 1991-12-18 | 1998-01-27 | Schering Corp | Imidazolyl or imidazolylalkyl substituted with a four or five membered nitrigen containing heterocyclic ring |
| GB9127304D0 (en) * | 1991-12-23 | 1992-02-19 | Boots Co Plc | Therapeutic agents |
| US5401851A (en) * | 1992-06-03 | 1995-03-28 | Eli Lilly And Company | Angiotensin II antagonists |
| US5612360A (en) * | 1992-06-03 | 1997-03-18 | Eli Lilly And Company | Angiotensin II antagonists |
| US5359073A (en) * | 1992-11-24 | 1994-10-25 | G. D. Searle & Co. | Substituted-phenyl (N,N'-cycloalkyl/alkyl carboxamide)-1H/3H-imidazo[4,5-b]pyridine compounds as PAF antagonists |
| US5262426A (en) * | 1993-01-22 | 1993-11-16 | G. D. Searle & Co. | N,N'-cycloalkyl/alkyl carboxamide 4H-imidazo-[4,5-b]pyridine compounds as PAF antagonists |
| US5360907A (en) * | 1993-06-14 | 1994-11-01 | G.D. Searle & Co. | Pyrrolo[3,2-B]pyridinylalkyl benzamide derivatives |
| GB9312893D0 (en) * | 1993-06-22 | 1993-08-04 | Boots Co Plc | Therapeutic agents |
| AU2199195A (en) * | 1994-04-28 | 1995-11-29 | Uniroyal Chemical Company, Inc. | Fungicidal azole derivatives |
| FR2723369B1 (en) * | 1994-08-02 | 1996-09-13 | Roussel Uclaf | NEW IMIDAZOLE DERIVATIVES, THEIR PREPARATION PROCESS, THE NEW INTERMEDIATES OBTAINED, THEIR APPLICATION AS MEDICAMENTS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
| FR2723370B1 (en) * | 1994-08-02 | 1996-09-13 | Roussel Uclaf | NEW IMIDAZOLE DERIVATIVES, THEIR PREPARATION PROCESS, THE NEW INTERMEDIATES OBTAINED, THEIR APPLICATION AS MEDICAMENTS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
| US5652363A (en) * | 1995-10-05 | 1997-07-29 | C.D. Searle & Co. | Pyrido-1,4-oxazinylalkyl-benzamide derivatives |
| FR2757511B1 (en) * | 1996-12-23 | 2001-05-04 | Sanofi Sa | PROCESS FOR THE PREPARATION OF A TETRAHYDROPYRIDINE DERIVATIVE |
| US5855869A (en) * | 1996-12-31 | 1999-01-05 | Rhodia Inc. | Microparticulate abrasives |
| WO2000069823A1 (en) * | 1999-05-12 | 2000-11-23 | Neurosearch A/S | Ion channel modulating agents |
| JP2002262119A (en) | 2001-02-28 | 2002-09-13 | Sharp Corp | Image processing apparatus, image processing method, machine-readable recording medium storing image processing program, and image processing program |
| WO2011136285A1 (en) * | 2010-04-27 | 2011-11-03 | 日本製紙株式会社 | Cell differentiation promoter and use of same |
| JP2013540145A (en) * | 2010-10-21 | 2013-10-31 | ウニベルシテート デス ザールランデス | Selective CYP11B1 inhibitor for the treatment of cortisol-dependent diseases |
| JP6316282B2 (en) | 2012-05-29 | 2018-04-25 | モメンティブ パフォーマンス マテリアルズ ゲーエムベーハー | Preparation of isocyanate silane |
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|---|---|---|---|---|
| DE488681C (en) * | 1927-02-27 | 1930-01-06 | I G Farbenindustrie Akt Ges | Process for the preparation of imidazole derivatives |
| DE1620362A1 (en) * | 1966-05-04 | 1970-04-02 | Shell Int Research | Process for the production of N-alkyl- or N-alkenylimidazoles |
| US3592826A (en) * | 1967-05-22 | 1971-07-13 | Union Carbide Corp | Imidazole catalysts for diketene reactions |
| GB1321701A (en) * | 1969-10-01 | 1973-06-27 | Continental Pharma | Amino-alcohols their salts and process for prepairing the same |
| IE34545B1 (en) * | 1969-10-01 | 1975-06-11 | Continental Pharma | Amino-alcohols,their salts and process for preparing the same |
| FR2115153A1 (en) * | 1970-11-30 | 1972-07-07 | Berlin Chemie Veb | 1-acyl-imidazoles - with antiviral activity |
| GB1364312A (en) * | 1972-01-25 | 1974-08-21 | Beecham Group Ltd | Biologically active imidazoles |
| FR2215153A5 (en) * | 1973-01-19 | 1974-08-19 | Cit Alcatel | |
| FR2249616A1 (en) * | 1973-10-31 | 1975-05-30 | Pepro | Fungicidal compositions contg 1-aralkyl benzimidazoles - for treatment of plants and seeds |
| JPS5437953B2 (en) * | 1974-04-25 | 1979-11-17 | ||
| US3927017A (en) * | 1974-06-27 | 1975-12-16 | Janssen Pharmaceutica Nv | 1-({62 -Aryl-{62 -R-ethyl)imidazoles |
| DE2533211A1 (en) * | 1975-07-24 | 1977-02-10 | Heumann Ludwig & Co Gmbh | Imidazole deriv. prepn. - by reacting iminoester or amidine or their salts with alpha-acylamino ketone in liquid ammonia |
| US4036975A (en) * | 1975-07-28 | 1977-07-19 | Xyntex (U.S.A) Inc. | 1-[2-(1-Adamantyl)-2-(R-thio)ethyl]imidazoles and 1-[2-(1-adamantyl)-2-(R-oxy)ethyl]imidazoles |
| US4118461A (en) * | 1975-12-18 | 1978-10-03 | Rohm And Haas Company | 1-Substituted aralkyl imidazoles |
| GB1533706A (en) * | 1976-03-01 | 1978-11-29 | Ici Ltd | Fungicidal imidazoles and 1,2,4-triazoles |
| US4150153A (en) * | 1977-05-13 | 1979-04-17 | Syntex (U.S.A.) Inc. | 1-(Naphthylethyl)imidazole derivatives |
| US4284641A (en) * | 1977-08-26 | 1981-08-18 | Burroughs Wellcome Co. | Pharmaceutically active imidazole derivatives |
-
1978
- 1978-11-02 EP EP78101294A patent/EP0003732B1/en not_active Expired
- 1978-11-02 DE DE7878101294T patent/DE2862340D1/en not_active Expired
-
1979
- 1979-01-29 MC MC791359A patent/MC1241A1/en unknown
- 1979-01-31 ZA ZA79412A patent/ZA79412B/en unknown
- 1979-01-31 EP EP79100289A patent/EP0003560B1/en not_active Expired
- 1979-01-31 DK DK41479A patent/DK41479A/en not_active Application Discontinuation
- 1979-01-31 GB GB7903452A patent/GB2018136B/en not_active Expired
- 1979-01-31 NZ NZ189520A patent/NZ189520A/en unknown
- 1979-01-31 ES ES477305A patent/ES477305A1/en not_active Expired
- 1979-01-31 IT IT47847/79A patent/IT1115800B/en active
- 1979-01-31 DE DE19792903653 patent/DE2903653A1/en not_active Withdrawn
- 1979-01-31 IL IL56556A patent/IL56556A/en unknown
- 1979-01-31 AU AU43808/79A patent/AU533272B2/en not_active Ceased
- 1979-01-31 GB GB8137257A patent/GB2098064B/en not_active Expired
- 1979-01-31 HU HU79WE594A patent/HU182629B/en unknown
- 1979-01-31 GR GR58227A patent/GR65609B/en unknown
- 1979-01-31 AT AT0070979A patent/AT372949B/en not_active IP Right Cessation
- 1979-01-31 FR FR7902450A patent/FR2416012A1/en active Granted
- 1979-01-31 JP JP1028479A patent/JPS54145665A/en active Pending
- 1979-01-31 CA CA000320640A patent/CA1146549A/en not_active Expired
- 1979-01-31 DE DE7979100289T patent/DE2966948D1/en not_active Expired
- 1979-01-31 BE BE193196A patent/BE873849A/en not_active IP Right Cessation
- 1979-01-31 PT PT7969165A patent/PT69165A/en unknown
- 1979-01-31 NL NL7900807A patent/NL7900807A/en not_active Application Discontinuation
- 1979-01-31 FI FI790314A patent/FI790314A7/en not_active Application Discontinuation
- 1979-01-31 CH CH94579A patent/CH643736A5/en not_active IP Right Cessation
- 1979-01-31 LU LU80863A patent/LU80863A1/en unknown
- 1979-01-31 IE IE177/79A patent/IE47649B1/en unknown
- 1979-01-31 SE SE7900834A patent/SE7900834L/en not_active Application Discontinuation
- 1979-09-19 FR FR7923318A patent/FR2429593A1/en active Granted
-
1981
- 1981-04-02 US US06/250,454 patent/US4416895A/en not_active Expired - Fee Related
- 1981-04-02 US US06/250,481 patent/US4528195A/en not_active Expired - Fee Related
-
1982
- 1982-11-30 CA CA000416728A patent/CA1162855A/en not_active Expired
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